rs2215379
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2215379(C;C) |
| Make rs2215379(C;T) |
| Make rs2215379(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 78421278 |
| Gene | MAGI2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2215379 |
| dbSNP (classic) | rs2215379 |
| ClinGen | rs2215379 |
| ebi | rs2215379 |
| HLI | rs2215379 |
| Exac | rs2215379 |
| Gnomad | rs2215379 |
| Varsome | rs2215379 |
| LitVar | rs2215379 |
| Map | rs2215379 |
| PheGenI | rs2215379 |
| Biobank | rs2215379 |
| 1000 genomes | rs2215379 |
| hgdp | rs2215379 |
| ensembl | rs2215379 |
| geneview | rs2215379 |
| scholar | rs2215379 |
| rs2215379 | |
| pharmgkb | rs2215379 |
| gwascentral | rs2215379 |
| openSNP | rs2215379 |
| 23andMe | rs2215379 |
| SNPshot | rs2215379 |
| SNPdbe | rs2215379 |
| MSV3d | rs2215379 |
| GWAS Ctlg | rs2215379 |
| GMAF | 0.253 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22649501
] Common Variants in MAGI2 Gene Are Associated with Increased Risk for Cognitive Impairment in Schizophrenic Patients
